Literature DB >> 14693124

Natural killer (NK) cells play a critical role in the early innate immune response to Chlamydophila abortus infection in mice.

A J Buendía1, C M Martínez, N Ortega, L Del Río, M R Caro, M C Gallego, J Sánchez, J A Navarro, F Cuello, J Salinas.   

Abstract

Chlamydophila abortus, the aetiological agent of ovine enzootic abortion, induces a strong inflammatory reaction that leads to the T helper cell (Th1) specific immune response necessary for the clearance of infection. Because the role of natural killer (NK) cells during the first stages of this response has received little attention, this study focused on determining the function of these cells in a mouse model of infection. The location of NK cells in the liver and spleen of infected mice was examined immunohistochemically with an anti-Ly49G monoclonal antibody. The number of NK cells increased during the infection both in spleen and liver. In subsequent experiments, an anti-asialo GM1 polyclonal antibody was injected to deplete the NK cells. NK-depleted mice showed a substantial increase in their susceptibility to C. abortus infection, with high mortality rates and an increased burden of bacteria in the liver. Histopathological studies showed that inflammatory foci, composed mainly of neutrophils, were greater in size and number in depleted mice, while numerous chlamydial inclusions were associated with the foci. Serum concentrations of IFN-gamma, a key cytokine in the control of C. abortus infection, were substantially reduced in the NK-depleted mice. To establish the relationship between NK cells and other components of the innate immune response, neutrophils were depleted with the RB6-8C5 antibody. These cells were shown to be crucial in the recruitment of NK cells to the inflammatory foci.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14693124     DOI: 10.1016/s0021-9975(03)00069-0

Source DB:  PubMed          Journal:  J Comp Pathol        ISSN: 0021-9975            Impact factor:   1.311


  7 in total

1.  Natural killer cells support the induction of protective immunity during dendritic cell-mediated vaccination against Leishmania major.

Authors:  Katharina A Remer; Bianca Roeger; Christine Hambrecht; Heidrun Moll
Journal:  Immunology       Date:  2010-12       Impact factor: 7.397

2.  Comparative evaluation of the protective efficacy of two formulations of a recombinant Chlamydia abortus subunit candidate vaccine in a mouse model.

Authors:  Qing Pan; Roshan Pais; Adaugo Ohandjo; Cheng He; Qing He; Yusuf Omosun; J U Igietseme; F O Eko
Journal:  Vaccine       Date:  2015-02-17       Impact factor: 3.641

Review 3.  Recent advances and public health implications for environmental exposure to Chlamydia abortus: from enzootic to zoonotic disease.

Authors:  Lauretta Turin; Sara Surini; Nick Wheelhouse; Mara Silvia Rocchi
Journal:  Vet Res       Date:  2022-05-31       Impact factor: 3.829

Review 4.  New tools to study the role of B cells in cytomegalovirus infections.

Authors:  Ari Waisman; Andrew L Croxford; Filiz Demircik
Journal:  Med Microbiol Immunol       Date:  2008-03-11       Impact factor: 3.402

5.  The innate interferon gamma response of BALB/c and C57BL/6 mice to in vitro Burkholderia pseudomallei infection.

Authors:  Ghee Chong Koo; Yunn-Hwen Gan
Journal:  BMC Immunol       Date:  2006-08-18       Impact factor: 3.615

6.  Chlamydia abortus Pmp18.1 Induces IL-1β Secretion by TLR4 Activation through the MyD88, NF-κB, and Caspase-1 Signaling Pathways.

Authors:  Qing Pan; Qiang Zhang; Jun Chu; Roshan Pais; Shanshan Liu; Cheng He; Francis O Eko
Journal:  Front Cell Infect Microbiol       Date:  2017-12-18       Impact factor: 5.293

7.  Cellular Basis for the Enhanced Efficacy of the Fms-Like Tyrosine Kinase 3 Ligand (FL) Adjuvanted VCG-Based Chlamydia abortus Vaccine.

Authors:  Shakyra Richardson; Fnu Medhavi; Tayhlor Tanner; Stephanie Lundy; Yusuf Omosun; Joseph U Igietseme; Darin Carroll; Francis O Eko
Journal:  Front Immunol       Date:  2021-06-24       Impact factor: 7.561

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.